MethodologyUsing genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species1 Nottingham Arabidopsis Stock Centre, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough, LE12 5RD, UK 2 Plant Sciences Division, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough, LE12 5RD, UK 3 Warwick HRI, University of Warwick, Wellesbourne, Warwick, CV35 9EF, UK
Plant Methods 2005, 1:10doi:10.1186/1746-4811-1-10
Additional filesAdditional File 1: An archive of the mean probe-set signals of all genes in P-starved versus control (P-replete) Brassica oleracea var. alboglabra cv. A12DHd. Raw data were analysed with the RMA pre-normalisation algorithm using the ATH1-121501 probe mask file (no probe selection) or a custom probe mask file. The custom probe mask files were generated by hybridising gDNA from B. oleracea to Affymetrix A. thaliana ATH-121501 GeneChip® arrays and selecting probe-pairs in which B. oleracea gDNA hybridisation intensity values were greater than 50, 100, 150, 200, 300,...1000. Signal intensities are estimates from total RNA extracted from the shoots of hydroponically-grown plants (n = 4) under P-deficient (raw) and P-replete (control) conditions. The P-values are derived from a one-way ANOVA using a Benjamini and Hochberg False Discovery Rate (0.05) multiple testing correction. Format: ZIP Size: 8.2MB Download file Additional File 2: An archive containing all of the Perl scripts necessary in order to produce new CDF files for use in analysing cross-species hybridisation results. Format: ZIP Size: 25KB Download file Additional File 3: (CDF_filtering script instructions.doc : DOC file). An instruction document containing details for using the scripts contained within 2. Format: DOC Size: 21KB Download file This file can be viewed with: Microsoft Word Viewer |





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